DE1016875B - High pressure lubricating oils - Google Patents
High pressure lubricating oilsInfo
- Publication number
- DE1016875B DE1016875B DEB39612A DEB0039612A DE1016875B DE 1016875 B DE1016875 B DE 1016875B DE B39612 A DEB39612 A DE B39612A DE B0039612 A DEB0039612 A DE B0039612A DE 1016875 B DE1016875 B DE 1016875B
- Authority
- DE
- Germany
- Prior art keywords
- lubricating oils
- sulfur
- high pressure
- pressure lubricating
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/02—Sulfurised compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/04—Elements
- C10M2201/043—Sulfur; Selenenium; Tellurium
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/108—Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/20—Containing nitrogen-to-oxygen bonds
- C10M2215/202—Containing nitrogen-to-oxygen bonds containing nitro groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/022—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of hydrocarbons, e.g. olefines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Es ist bekannt, Hochdruckschmieröle herzustellen, indem man Schmierölen aromatische Nitroverbindungen zusammen mit Schwefel zugibt. Ferner ist bekannt, als Zusätze für Schmieröle Gemische aus aromatischen Nitroverbindungen neben Umsetzungsprodukten von Olefinen mit Schwefel oder auch solche aromatische Nitroverbindungen zu verwenden, die gleichzeitig ein oder mehrere zweiwertige Schwefelatome am aromatischen Rest gebunden enthalten.It is known to produce high pressure lubricating oils by adding aromatic nitro compounds to lubricating oils added together with sulfur. It is also known to use mixtures of aromatic oils as additives for lubricating oils Nitro compounds in addition to reaction products of olefins with sulfur or also those aromatic To use nitro compounds which simultaneously have one or more divalent sulfur atoms on the aromatic Rest bound included.
Es wurde nun gefunden, daß man besonders gute Hochdruckschmieröle erhält, wenn man Schmierölen auf Kohlenwasserstoffbasis oder Nichtkohlenwasserstoffbasis ein bei Temperaturen oberhalb 130°, zweckmäßig zwischen 150 und 200°, gewonnenes Umsetzungsprodukt aus 1, 2, 4-Trichlor-5-nitrobenzol, Styrol und elementarem Schwefel zugibt. Diese Umsetzungsprodukte enthalten den Schwefel nicht am aromatischen Kern gebunden, sondern an die olefinische Doppelbindung angelagert. Die zugesetzten Mengen des genannten Umsetzungsproduktes sollen 0,1 bis 10 Gewichtsprozent betragen; im allgemeinen sind Mengen zwischen 0,5 und 5 Gewichtsprozent ausreichend. It has now been found that particularly good high-pressure lubricating oils are obtained when lubricating oils are used Hydrocarbon-based or non-hydrocarbon-based one at temperatures above 130 °, expedient between 150 and 200 °, obtained reaction product from 1, 2, 4-trichloro-5-nitrobenzene, styrene and elemental Admits sulfur. These reaction products do not contain the sulfur bound to the aromatic nucleus, but attached to the olefinic double bond. The added amounts of the reaction product mentioned should be 0.1 to 10 percent by weight; in general, amounts between 0.5 and 5 percent by weight are sufficient.
Als vorteilhaft hat sich herausgestellt, bei der Umsetzung von 1,2, 4-Trichlor-5-nitrobenzol, Styrol und elementarem Schwefel molare Mengen anzuwenden, da hierbei ein bei normaler Temperatur flüssiges Reaktionsprodukt erhalten wird, das leicht in den zu verbessernden Schmierölen gelöst werden kann. Bei Anwendung anderer Mengenverhältnisse erhält man ein Gemisch aus flüssigen und festen Anteilen, das sich weniger gut in den Schmierölen löst, aus dem aber die festen Anteile verhältnismäßig leicht abgetrennt werden können.It has been found to be advantageous in the implementation of 1,2,4-trichloro-5-nitrobenzene, styrene and molar amounts of elemental sulfur to be used, since this gives a reaction product which is liquid at normal temperature and which can easily be improved in the Lubricating oils can be dissolved. If other proportions are used, a mixture of liquids is obtained and solid fractions, which dissolve less well in lubricating oils, but from which the solid fractions are proportionately can be easily separated.
Man legt in einem Rührkolben 100 Gewichtsteile Schwefel vor und gibt bei 160 bis 170° langsam eine feine pulvrige Aufschlämmung von 226 Gewichtsteilen 1,2,4-Trichlor-5-nitrobenzol zu. Nach 3 bis 4 Stunden bei 160 bis 170° erhält man ein bei Normaltemperaturen braun gefärbtes flüssiges Umsetzungsprodukt, das rückstandslos filtrierbar ist. Es enthält 19,5 Gewichtsprozent Schwefel, 2,4 Gewichtsprozent Stickstoff und 20,6 Gewichtsprozent Chlor. Gibt man 0,1 bis 10 Gewichtsprozent dieser Flüssigkeit zu Mineralölen oder zu Schmierölen mit polaren Gruppen, so erhält man z. B. bei 4°/0igem Zusatz die in der nachstehenden Tabelle im Vierkugelapparat ermittelten Ergebnisse.100 parts by weight of sulfur are placed in a stirred flask and a fine powdery suspension of 226 parts by weight of 1,2,4-trichloro-5-nitrobenzene is slowly added at 160 ° to 170 °. After 3 to 4 hours at 160 to 170 °, a liquid reaction product which is brown in color at normal temperatures and which can be filtered without leaving any residue is obtained. It contains 19.5 percent by weight sulfur, 2.4 percent by weight nitrogen and 20.6 percent by weight chlorine. If 0.1 to 10 percent by weight of this liquid is added to mineral oils or to lubricating oils with polar groups, z. B. at 4 ° / 0 sodium addition the results determined in the following table in the four-ball apparatus.
Aus den angeführten Zahlen ist ferner ersichtlich, daß das bei der Umsetzung der genannten drei Stoffe erhaltene Reaktionsprodukt bei der Zugabe zu Schmierölen eine bessere Wirkung zeigt als die Mischung der drei Komponenten (vgl. Versuch 5).It can also be seen from the figures quoted that this is obtained when the three substances mentioned are reacted Reaction product when added to lubricating oils shows a better effect than the mixture of the three components (see experiment 5).
Ferner ist ersichtlich, daß das beanspruchte Reaktionsprodukt auch dem bekannten Zusatz von Gemischen aus It can also be seen that the claimed reaction product also consists of the known addition of mixtures
Anmelder:Applicant:
Badische Anilin- & Soda-Fabrik Aktiengesellschaft, Ludwigshafen/RheinBadische Anilin- & Soda-Fabrik Aktiengesellschaft, Ludwigshafen / Rhein
Dr. Adolf Hrubesch, Ludwigshafen/Rhein, ist als Erfinder genannt wordenDr. Adolf Hrubesch, Ludwigshafen / Rhein, has been named as the inventor
aromatischen Nitroverbindungen mit Umsetzungsprodukten von Olefinen mit Schwefel überlegen ist (vgl. Versuche 6 bis 9).is superior to aromatic nitro compounds with reaction products of olefins with sulfur (cf. Trials 6 to 9).
1. Polyglykoläther1. Polyglycol ether
2. Polyglykoläther + 4%
erfindungsgemäßerZusatz2. polyglycol ether + 4%
additive according to the invention
3. Mineralöl SAE 203. Mineral oil SAE 20
4. Mineralöl SAE 20 + 4%4. Mineral oil SAE 20 + 4%
erfindungsgemäßerZusatzadditive according to the invention
5. Mineralöl SAE 20 + 1,6%5. Mineral oil SAE 20 + 1.6%
Styrol+ 1,6% 1,2,4-Tri-Styrene + 1.6% 1,2,4-tri-
chlor-5-nitrobenzolchloro-5-nitrobenzene
+ 0,8% Schwefel + 0.8% sulfur
6. Mineralöl SAE 20 + 4%6. Mineral oil SAE 20 + 4%
o-Chlornitrobenzol + 2 %
geschwefeltes Styrol,o-chloronitrobenzene + 2%
sulphurized styrene,
22,8% Schwefel22.8% sulfur
7. Mineralöl SAE 20 + 4%7. Mineral oil SAE 20 + 4%
o-Chlornitrobenzol
+2 % Terpentinsulfid ..o-chloronitrobenzene
+ 2% turpentine sulfide ..
8. Mineralöl SAE 20 + 4%8. Mineral oil SAE 20 + 4%
2, 4-Dinitrophenol + 2%
geschwefeltes Styrol,2,4-Dinitrophenol + 2%
sulphurized styrene,
22,8% Schwefel22.8% sulfur
9. Mineralöl SAE 20 + 4%
p-Nitrobenzophenon
+ 2% geschwefeltes
Styrol, 22,8% Schwefel..9. Mineral oil SAE 20 + 4%
p-nitrobenzophenone
+ 2% sulphurized
Styrene, 22.8% sulfur ..
Freßbelastung Feeding stress
kgkg
150150
800 160800 160
900900
700700
650650
260260
300300
320320
Durchmesserdiameter
derthe
Verschleißkalotte Wear cap
2,12.1
2,5 2,12.5 2.1
2,62.6
3,03.0
3,8 3,03.8 3.0
3,03.0
3,13.1
709 699086709 699086
3 43 4
Die erfindungsgemäß erhaltenen Schmieröle stellen Öle prozent an einem bei Temperaturen oberhalb 130°The lubricating oils obtained according to the invention represent oils in percent at temperatures above 130 °
von der Qualität der Hypoidöle dar. gewonnenen Umsetzungsprodukt aus 1, 2, 4-Trichlor-of the quality of the hypoid oils. Reaction product obtained from 1, 2, 4-trichloro
5-nitrobenzol, Styrol und elementarem Schwefel.5-nitrobenzene, styrene and elemental sulfur.
Claims (1)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB39612A DE1016875B (en) | 1956-03-22 | 1956-03-22 | High pressure lubricating oils |
FR1169905D FR1169905A (en) | 1956-03-22 | 1957-03-21 | Lubricants for high pressures |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB39612A DE1016875B (en) | 1956-03-22 | 1956-03-22 | High pressure lubricating oils |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1016875B true DE1016875B (en) | 1957-10-03 |
Family
ID=6965852
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEB39612A Pending DE1016875B (en) | 1956-03-22 | 1956-03-22 | High pressure lubricating oils |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1016875B (en) |
FR (1) | FR1169905A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB455305A (en) * | 1934-04-24 | 1936-10-19 | Du Pont | Improvements in or relating to lubricants |
DE926680C (en) * | 1952-08-25 | 1955-04-21 | Huels Chemische Werke Ag | Additives for lubricants |
-
1956
- 1956-03-22 DE DEB39612A patent/DE1016875B/en active Pending
-
1957
- 1957-03-21 FR FR1169905D patent/FR1169905A/en not_active Expired
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB455305A (en) * | 1934-04-24 | 1936-10-19 | Du Pont | Improvements in or relating to lubricants |
DE926680C (en) * | 1952-08-25 | 1955-04-21 | Huels Chemische Werke Ag | Additives for lubricants |
Also Published As
Publication number | Publication date |
---|---|
FR1169905A (en) | 1959-01-07 |
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